A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15924258



Internal ID2481604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68872875..68941954hg38UCSC Ensembl
chr18:66540112..66609191hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3869080
hg1969080
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642955
Supporting Variants
SamplesHG02185
Known GenesCCDC102B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15924258
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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